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1-(3,5-bis-trifluoromethyl-benzyl)-5-chloro-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

620534-09-0

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  • 1-(3,5-bis-trifluoromethyl-benzyl)-5-chloro-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester

    Cas No: 620534-09-0

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  • 1-(3,5-bis-trifluoromethyl-benzyl)-5-chloro-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester

    Cas No: 620534-09-0

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620534-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620534-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,5,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 620534-09:
(8*6)+(7*2)+(6*0)+(5*5)+(4*3)+(3*4)+(2*0)+(1*9)=120
120 % 10 = 0
So 620534-09-0 is a valid CAS Registry Number.

620534-09-0Relevant articles and documents

Pyridine metallations in the synthesis of triazole based NK-1 antagonists

Jeff Thrasher,Hembre, Erik J.,Gardinier, Kevin M.,Savin, Kenneth A.,Hong, Jian Eric,Jungheim, Louis N.

, p. 543 - 547 (2006)

Regioselective pyridine metallation chemistry was used to produce N-(3-chloropyridin-4-ylmethyl)-N-methyl-1-(3,5-bis-trifluoromethylbenzyl)-5-phenyl-1H-[1,2,3]triazole-4-carboxamide (9a) and [1-(3,5-bis-trifluoromethyl-benzyl)-5-morpholin-4-yl-1H-[1,2,3]t

TACHYKININ RECEPTOR ANTAGONISTS

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Page 42, (2010/02/10)

The present invention relates to selective NK-1 receptor antagonists of Formula (I) or a pharmaceutically acceptable salt thereof, for the treatment of disorders associated with an excess of tachykinins.

TRIAZOLE DERIVATIVES AS TACHYKININ RECEPTOR ANTAGONISTS

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Page/Page column 53, (2010/02/07)

This application relates to a compound of Formula (I) or a pharmaceutically acceptable salt thereof, pharmaceutical compositions thereof, and its use as an inhibitor of the NK-1 subtype of tachykinin receptors, as well as a process for its preparation and intermediates therefor. (I) wherein: D is a C1-C3 alkane-diyl; R1 is phenyl, which is optionally substituted with one to three substitutents indpendently selected from the group consisting of halo, C1-C4 alkyl, C1-C4 alkoxy, cyano, difluoromethyl, trifluoromethyl, and trifluoromethoxy; R4 is a radical selected from the group consisting of: (IA), (IB), (IC), (ID), (IE), (IF), (IG), (IH)

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